ComplianceOnline

US FDA 510(k): Best Practices for 510(k) Preparation and Submission

Instructor: David Lim 
Product ID: 703218
Training Level: Intermediate
  • Duration: 60 Min

recorded version

$229.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jan-2014

Training CD / USB Drive

$299.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar will discuss best practices for premarket notification [510(k)] preparation and submission compliant with FDA's eCopy and Refuse to Accept (RTA) Policy requirements.

Why Should You Attend:

Although it is believed there are various factors contributing to timing of 510(k) clearances, it is imperative more than ever from our industry perspectives that the medical device manufacturers understand recent changes (hurdles and new requirements) and be able to prepare a 510(k) in a sufficiently adequate way to expedite the review process and successful clearance without delays, saving an enormous amount of time, energy, and resources.

In this webinar, speaker will discuss how to put together a compelling 510(k) package. In particular, the speaker will share what he has observed and learned from his own experience and also based on his analysis of 510(k)s recently cleared.

This 60-minute webinar will provide great opportunity to implement your good practices for a 510(k) preparation and submission while meeting eCopy and RTA policy requirements necessary for obtaining 510(k) clearances.

Areas Covered in the webinar:

  • Statute(s) and regulations governing 510(k)s
  • Definitions and medical device classification including IVD devices
  • Intended use, indications, and predicates
  • eCopy program
  • Refuse to accept (RTA) policy
  • Standards - benefits
  • Who/when is required to submit a 510(k)
  • Regulatory requirements: performance testing and/or clinical data
  • 510(k) content and format
  • How to increase 510(k) submission quality for a product.
  • Responding to FDA’s request of additional information.
  • Resolving different opinions between the submitter and FDA reviewer(s)
  • Good practices: Dos and Don’ts including de novo process
  • Conclusion

Who Will Benefit:

  • Regulatory affairs (associates, specialists, managers, directors or VPs)
  • Quality professionals (associates, specialists, managers, directors or VPs)
  • R&D (engineers, scientists, managers, directors or VPs)
  • Complaint and risk management personnel
  • Consultants
  • Contractors/subcontractors
  • CEOs
  • VPs
  • Clinical affairs (associates, specialists, managers, directors or VPs)

Instructor Profile:

Dr. David Lim, Ph.D., RAC, ASQ-CQA. Dr. Lim is President and Principal of Regulatory Doctor. Dr. Lim frequently presents global regulatory and quality compliance topics in various forums and meetings. Recently, Dr. Lim developed 510(k) templates ready for use, compliant with e-Copy and RTA policy. In addition, Dr. Lim developed FDA inspection checklists for drug and medical device manufacturers based on his analysis of FDA inspectional observations cited in 483s for the past seven years. Dr. Lim provides his feedback to regulatory agency (e.g., US FDA) through public comments and also served as a panel member during the FDA’s transparency public meeting in 2009. Dr. Lim contributes to the Regulatory Affairs Professional Society (RAPS) as an author and speaker. Dr. Lim leads and directs all research projects including pharmacovigilance, medical device reporting, recalls and patient safety signals being conducted at the Regulatory Doctor.

Follow us :
Upcoming In-person Seminars by EX-FDA OFFICIALS
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed
    Loading